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actiCHARGE

EUDAMED

Class I (EU MDR)

Ref SBM1AF100

by Sublimed

Identity

Trade Name
actiCHARGE EUDAMED
Device Name
actiCHARGE EUDAMED
Model / Reference
SBM1AF100 EUDAMED

Identifiers

Primary DI / UDI-DI
03770018808147 EUDAMED
Basic UDI-DI
3770018808actiCHARGE1DL EUDAMED
Direct Marketing DI
03770018808147 EUDAMED
EMDN Code
Z120601 ELECTROTHERAPY EQUIPMENT (INCLUDED TENS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

actiCHARGE by Sublimed — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Sublimed
EUDAMED SRN
FR-MF-000007546

Sources (1)

  • EUDAMED c0753887-b420-495d-8c40-03e5b718494a 61 fields · synced Jul 13, 2026